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Many glycoproteins of lower and higher eucaryotes are attached to the plasma membrane by means of a glycosylphosphatidylinositol .

很多高等和低等真核生物的糖蛋白是以糖基磷脂酰肌醇锚定的方式被连接在质膜上。

Many glycoproteins of lower and higher eucaryotes are attached to the plasma membrane by means of a glycosylphosp...

很多高等和低等真核生物的糖蛋白是以糖基磷脂酰肌醇锚定的方式被连接在质膜上。

These results suggested that phosphatidylcholine probably was the plasma membrane target for Fengycins.

这些结果说明卵磷脂很可能是Fengycins在膜上的作用靶标。

There was no significant difference of satuate phosphatidylcholine level between every group and every time point of each group.

显示CPB在术中和术后早期并无显著影响PS中磷脂的主要活性成分。

NgR has emerged as a focal point of convergence for mediating growth-inhibitory activities.

NgR是中枢神经元细胞膜上的一种蛋白,该蛋白和p75NTR及LINGO-1这两种中枢神经元细胞膜蛋白组成复合受体,介导了中枢神经系统髓磷脂中MAG、OMgp、Nogo对中枢神经元轴突生长的抑制作用,从而造成了成年哺乳动物中枢神经损伤后再生困难。

AIM: To develop a supercritical fluid extraction method for the phospholipids of Polygonum multiflorum Thunb.

目的:建立超临界流体萃取中药何首乌中的磷脂类成分的方法。

Cellulose, potassium bicarbonate, modified cellulose gum, modified cellulose, magnesium stearate, soy lecithin, and carnauba wax.

纤维素,碳酸氢钾,改性纤维素胶,改性纤维素,硬脂酸镁,大豆卵磷脂,和巴西棕榈蜡。

Reports of the relative potency of these growth factors and the ability of heparin to potentiate the activity of bFGF are conflicting.

这些生长因素的相对的力气和增强的肝磷脂的能力的报告bFGF的活动是相冲突的。

Methods SH-SY5Y cells, a human neuroblastoma cell line, were incubated with different concentrations of fluoride for 48 hr and somle of them were treated with vitamin E precedently. The functional situation of cells was measured by MTT method; lipid peroxidation was detected by High-Performance Liquid Chromatography; phospholipid was separated by a Silica SepPak cartridge and neutral lipids by HPLC.

体外培养SH-SY5Y人脑神经母细胞瘤细胞,在培养液中加入不同浓度的氟化物或加入抗氧化剂,培养48h后用测定细胞MTT的方法来了解细胞的损伤程度,用高效液相色谱法分离和测定培养液中脂质过氧化物水平,用过柱和比色法测定细胞生物膜磷脂含量,用高效液相色谱法测定细胞生物膜辅酶Q和胆固醇含量。

After tail iv injection, the blood exposure time of stealth liposomes and the area under blood drug concentration-time curve were pronouncedly increased, compared with the regular liposomes group and the free doxorubicin group,respectively.

以化学梯度法包封脂质体,用两亲性聚乙二醇-二硬脂酰磷脂酰乙醇胺对脂质体膜进行修饰以制备隐形脂质体;用HPLC-UV法测定给药后小鼠体内组织中的药物浓度。

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